TRIM77

gene
On this page

Summary

TRIM77 (tripartite motif containing 77, HGNC:34228) is a protein-coding gene on chromosome 11q14.3, encoding Tripartite motif-containing protein 77 (I1YAP6).

Predicted to enable ubiquitin protein ligase activity. Predicted to be involved in innate immune response and regulation of gene expression. Predicted to be active in cytoplasm.

Source: NCBI Gene 390231 — RefSeq curated summary.

At a glance

  • GWAS associations: 2
  • Clinical variants (ClinVar): 80 total
  • MANE Select transcript: NM_001146162

Identifiers

Gene identifiers

FieldValue
HGNC IDHGNC:34228
Approved symbolTRIM77
Nametripartite motif containing 77
Location11q14.3
Locus typegene with protein product
StatusApproved
Ensembl geneENSG00000214414
Ensembl biotypeprotein_coding
Entrez390231

Gene structure

Transcript identifiers

Ensembl transcripts: 2 — 2 protein_coding

ENST00000398290, ENST00000534392

RefSeq mRNA: 2 — MANE Select: NM_001146162 NM_001146162, NM_001271942

CCDS: CCDS60929

Canonical transcript exons

ENST00000398290 — 6 exons

ExonStartEnd
ENSE000015325168971141089711505
ENSE000015325188971029989710709
ENSE000036841198971737989717872
ENSE000037577208971515889715180
ENSE000037601698971589089715987
ENSE000037602608971419289714422

Expression profiles

Bgee: expression breadth tissue_specific, 2 present calls, max score 57.57.

Top tissues by expression

129 total, by Bgee expression score (0-100, higher = more expressed):

TissueAnatomy IDExpression scoreQuality
primordial germ cell in gonadCL:0000670 ∩ UBERON:000099157.57silver quality
colonic epitheliumUBERON:000039737.20gold quality
sural nerveUBERON:001548837.14gold quality
ventricular zoneUBERON:000305336.48gold quality
cortical plateUBERON:000534336.47gold quality
bone marrow cellCL:000209236.16gold quality
ganglionic eminenceUBERON:000402335.49gold quality
skeletal muscle tissueUBERON:000113433.38gold quality
hindlimb stylopod muscleUBERON:000425232.15gold quality
bone marrowUBERON:000237131.74gold quality
muscle tissueUBERON:000238531.06gold quality
liverUBERON:000210730.30gold quality
prefrontal cortexUBERON:000045129.89gold quality
stromal cell of endometriumCL:000225529.87gold quality
corpus callosumUBERON:000233628.99gold quality
monocyteCL:000057628.40gold quality
leukocyteCL:000073828.33gold quality
duodenumUBERON:000211428.14gold quality
lymph nodeUBERON:000002927.57gold quality
superior frontal gyrusUBERON:000266127.50gold quality
tonsilUBERON:000237227.05gold quality
islet of LangerhansUBERON:000000626.55gold quality
vermiform appendixUBERON:000115426.42gold quality
bloodUBERON:000017826.04gold quality
gall bladderUBERON:000211025.98gold quality
olfactory segment of nasal mucosaUBERON:000538625.89gold quality
placentaUBERON:000198725.81gold quality
urinary bladderUBERON:000125525.72gold quality
right lobe of liverUBERON:000111424.84gold quality
muscle of legUBERON:000138324.74gold quality

Single-cell (SCXA)

Detected in 1 experiment(s), a significant marker in 0.

ExperimentMarker?Max mean expression
E-ANND-3no2.12

Regulation

Is transcription factor: no

Cross-species orthologs

0 orthologs

Paralogs (80): MID2 (ENSG00000080561), TRIM9 (ENSG00000100505), MID1 (ENSG00000101871), MEFV (ENSG00000103313), TRIM35 (ENSG00000104228), TRIM14 (ENSG00000106785), TRIM37 (ENSG00000108395), TRIM2 (ENSG00000109654), TRIM3 (ENSG00000110171), TRIM38 (ENSG00000112343), TRIM62 (ENSG00000116525), TRIM67 (ENSG00000119283), TRIM32 (ENSG00000119401), BSPRY (ENSG00000119411), TRIM25 (ENSG00000121060), TRIM6 (ENSG00000121236), TRIM24 (ENSG00000122779), TRIM51 (ENSG00000124900), TRIM28 (ENSG00000130726), TRIM21 (ENSG00000132109), TRIM5 (ENSG00000132256), TRIM22 (ENSG00000132274), TRIM47 (ENSG00000132481), TRIM45 (ENSG00000134253), TRIM29 (ENSG00000137699), TRIM54 (ENSG00000138100), PML (ENSG00000140464), TRIM65 (ENSG00000141569), TRIM43B (ENSG00000144010), TRIM43 (ENSG00000144015), TRIM7 (ENSG00000146054), TRIM41 (ENSG00000146063), TRIM50 (ENSG00000146755), TRIM4 (ENSG00000146833), TRIM55 (ENSG00000147573), TRIM48 (ENSG00000150244), TRIM36 (ENSG00000152503), TRIM11 (ENSG00000154370), TRIM74 (ENSG00000155428), TRIM42 (ENSG00000155890)

Protein

Protein identifiers

Tripartite motif-containing protein 77I1YAP6 (reviewed: I1YAP6)

All UniProt accessions (2): I1YAP6, S4R3H6

UniProt curated annotations — full annotation on UniProt →

Similarity. Belongs to the TRIM/RBCC family.

RefSeq proteins (2): NP_001139634, NP_001258871 (=MANE)

Domains & families (InterPro)

IDNameType
IPR000315Znf_B-boxDomain
IPR001841Znf_RINGDomain
IPR001870B30.2/SPRYDomain
IPR003877SPRY_domDomain
IPR003879Butyrophylin_SPRYDomain
IPR013083Znf_RING/FYVE/PHDHomologous_superfamily
IPR013320ConA-like_dom_sfHomologous_superfamily
IPR017907Znf_RING_CSConserved_site
IPR018957Znf_C3HC4_RING-typeDomain
IPR043136B30.2/SPRY_sfHomologous_superfamily
IPR050143TRIM/RBCCFamily

Pfam: PF00097, PF00622

UniProt features (8 total): binding site 4, zinc finger region 2, chain 1, domain 1

Structure

Experimental structures (PDB)

0 structures.

Predicted structure (AlphaFold)

ModelpLDDTFraction very-high
AF-I1YAP6-F182.100.40

Functional residue map

Curated UniProt residues grouped by drug-discovery relevance — catalytic, ligand-binding, modification, and mutation-validated positions. Source: UniProtKB sequence features.

Ligand- & substrate-binding residues (4): 93; 96; 115; 121

Function

Pathways and Gene Ontology

Reactome pathways

0 pathways

MSigDB gene sets: 6 (showing top): GOBP_DEFENSE_RESPONSE_TO_OTHER_ORGANISM, GOMF_ACYLTRANSFERASE_ACTIVITY, GOMF_AMINOACYLTRANSFERASE_ACTIVITY, GOMF_UBIQUITIN_LIKE_PROTEIN_LIGASE_ACTIVITY, chr11q14, GOBP_BIOLOGICAL_PROCESS_INVOLVED_IN_INTERSPECIES_INTERACTION_BETWEEN_ORGANISMS

GO Biological Process (2): regulation of gene expression (GO:0010468), innate immune response (GO:0045087)

GO Molecular Function (4): zinc ion binding (GO:0008270), ubiquitin protein ligase activity (GO:0061630), protein binding (GO:0005515), metal ion binding (GO:0046872)

GO Cellular Component (1): cytoplasm (GO:0005737)

GO top-level categories

Rollup of top GO terms by namespace:

CategoryTerms
gene expression1
regulation of macromolecule biosynthetic process1
immune response1
defense response to symbiont1
transition metal ion binding1
ubiquitin-protein transferase activity1
ubiquitin-like protein ligase activity1
binding1
cation binding1
intracellular anatomical structure1
cellular anatomical structure1

Protein interactions and networks

STRING

202 interactions, top by confidence (×1000):

Protein AProtein BPartner UniProtScore
TRIM77TRIM42Q8IWZ5502
TRIM77FAM153AQ9UHL3480
TRIM77ZNF396Q96N95473
TRIM77TRIM52Q96A61421
TRIM77TRIM55Q9BYV6419
TRIM77TRIM59Q8IWR1404
TRIM77TRIM14Q14142370
TRIM77ANKRD20A4PQ4UJ75353
TRIM77TRIM23P36406348
TRIM77TRIM67Q6ZTA4324
TRIM77TRIM47Q96LD4322
TRIM77FRG1Q14331311
TRIM77TRIM54Q9BYV2293
TRIM77TRIM56Q9BRZ2293
TRIM77TRIM74Q86UV6278

IntAct

2 interactions, top by confidence:

ABTypeScore
TRIM77H2BC5psi-mi:“MI:0915”(physical association)0.400

BioGRID (1): HIST1H2BD (Proximity Label-MS)

ESM2 similar proteins: A0A3B3IT33, A6NCK2, A6NDI0, A6NGJ6, A6NI03, A6NLI5, C9J1S8, I1YAP6, K7N6K2, P0CI25, P0CI26, P15533, Q0PF16, Q1ACD5, Q1ACD6, Q1ACD7, Q1ACD8, Q2YEM8, Q2YEM9, Q2YEN0, Q2YEN2, Q3ZEE5, Q587N6, Q587N7, Q5BN31, Q5C8T6, Q5C8T8, Q5C8U1, Q5C8U3, Q5C8U4, Q5D7H7, Q5D7H8, Q5D7I0, Q5D7I1, Q5D7I2, Q5D7I3, Q5D7I5, Q5D7I6, Q5D7I9, Q5D7J0

Diamond homologs: A0A3B3IT33, A6NCK2, A6NDI0, A6NGJ6, A6NI03, A6NLI5, B0BLU1, C9J1S8, I1YAP6, O00478, O00481, O15344, O75677, O75678, O75679, O76064, P0CI25, P0CI26, P18892, P19474, P62603, P86448, P86449, Q13410, Q2HJ46, Q3C1V9, Q3TL54, Q4KLN8, Q5EBN2, Q5PQN2, Q5R4I2, Q5R996, Q61510, Q62556, Q6INS5, Q6MFY8, Q6UX41, Q6UXE8, Q6ZWI9, Q7T308

SIGNOR signaling

1 interactions.

AEffectBMechanism
Ub:E2“up-regulates activity”TRIM77ubiquitination

Disease & clinical

Clinical variants and AI predictions

ClinVar

80 variants total. Per-class counts are floors (≥ shown; pagination cap):

ClassificationCount (floor)
Pathogenic0
Likely pathogenic0
Uncertain significance78
Likely benign2
Benign0

Top pathogenic / likely-pathogenic (0)

SpliceAI

920 predictions. Top by Δscore:

VariantEffectΔscore
11:89711501:GGGAA:Gdonor_gain1.0000
11:89711502:GGAAG:Gdonor_gain1.0000
11:89711503:G:GTdonor_gain1.0000
11:89711503:G:Tdonor_gain1.0000
11:89711506:G:GGdonor_gain1.0000
11:89711510:GCA:Gdonor_gain1.0000
11:89711513:G:GGdonor_gain1.0000
11:89715884:TTGCA:Tacceptor_loss1.0000
11:89715885:TGCA:Tacceptor_loss1.0000
11:89715888:A:AGacceptor_gain1.0000
11:89715888:A:Gacceptor_loss1.0000
11:89715888:AG:Aacceptor_gain1.0000
11:89715889:G:GGacceptor_gain1.0000
11:89715889:G:GTacceptor_loss1.0000
11:89715889:GG:Gacceptor_gain1.0000
11:89715889:GGA:Gacceptor_gain1.0000
11:89715889:GGAAT:Gacceptor_gain1.0000
11:89715985:GAG:Gdonor_gain1.0000
11:89715986:AGG:Adonor_loss1.0000
11:89711502:GGAA:Gdonor_gain0.9900
11:89711503:GAA:Gdonor_gain0.9900
11:89715889:GGAA:Gacceptor_gain0.9900
11:89717137:G:GGdonor_gain0.9900
11:89717377:A:AGacceptor_gain0.9900
11:89717378:G:GGacceptor_gain0.9900
11:89717378:GT:Gacceptor_gain0.9900
11:89717378:GTGT:Gacceptor_gain0.9900
11:89711408:A:AGacceptor_gain0.9800
11:89711409:G:GGacceptor_gain0.9800
11:89717136:A:AGdonor_gain0.9800

AlphaMissense

3018 scored. Top likely-pathogenic:

VariantProtein changeam_pathogenicity
11:89717777:T:CF420L0.975
11:89717779:T:AF420L0.975
11:89717779:T:GF420L0.975
11:89717747:T:CF410L0.970
11:89717749:C:AF410L0.970
11:89717749:C:GF410L0.970
11:89717548:G:CW343C0.964
11:89717548:G:TW343C0.964
11:89717546:T:AW343R0.959
11:89717546:T:CW343R0.959
11:89717576:T:AW353R0.957
11:89717576:T:CW353R0.957
11:89717849:T:CF444L0.947
11:89717851:C:AF444L0.947
11:89717851:C:GF444L0.947
11:89717586:G:AG356E0.941
11:89717774:A:CS419R0.936
11:89717776:C:AS419R0.936
11:89717776:C:GS419R0.936
11:89717645:T:CF376L0.933
11:89717647:T:AF376L0.933
11:89717647:T:GF376L0.933
11:89717778:T:CF420S0.929
11:89717547:G:CW343S0.917
11:89717543:T:GY342D0.916
11:89710398:T:CF34L0.912
11:89710400:T:AF34L0.912
11:89710400:T:GF34L0.912
11:89717578:G:CW353C0.912
11:89717578:G:TW353C0.912

dbSNP variants (sampled 300 via entrez): RS1000428182 (11:89717023 T>C), RS1000574934 (11:89712321 C>T), RS1001033665 (11:89718235 G>A,C,T), RS1001147514 (11:89717274 T>C), RS1001374289 (11:89717601 C>G), RS1001416271 (11:89711327 C>G), RS1002363746 (11:89712403 A>G), RS1002823162 (11:89712719 T>G), RS1003415426 (11:89714131 C>T), RS1004547371 (11:89717935 T>G), RS1004654719 (11:89711651 T>C), RS1004770625 (11:89711363 A>G), RS1005654692 (11:89713127 C>A), RS1005770807 (11:89712777 G>A), RS1007988683 (11:89708631 G>A,C)

Disease associations

OMIM: gene `` | disease phenotypes:

GenCC curated gene-disease

Mondo (0):

Orphanet (0):

HPO phenotypes

0 total (0 of 0 shown, HPO-id order):

GWAS associations

2 associations (top):

StudyTraitp-value
GCST007998_24Intraocular pressure3.000000e-07
GCST012020_222Serum metabolite levels6.000000e-20

EFO canonical traits (1, from GWAS)

EFO IDTrait name
EFO:0004695intraocular pressure measurement

Drugs & pharmacology

Drug and pharmacology data

Is drug target: no

PharmGKB: 1 entry (VIP=true, CPIC=false)

CTD chemical–gene interactions

1 total (human), top 1 by PubMed support.

ChemicalActions (top 5)PubMed papers
Aflatoxin B1decreases methylation1

Clinical trials (associated diseases)

0 trials via MONDO — disease-level, not drug-specific.

No linked Atlas pages yet — the cross-entity mesh grows as the corpus expands.